Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80055
Gene Symbol: PGAP1
PGAP1 		0.600 Biomarker disease GENOMICS_ENGLAND Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline. 26050939 2015
Entrez Id: 80055
Gene Symbol: PGAP1
PGAP1 		0.600 GeneticVariation disease CLINVAR PGAP1 knock-out mice show otocephaly and male infertility. 17711852 2007
Entrez Id: 80055
Gene Symbol: PGAP1
PGAP1 		0.600 CausalMutation disease CLINVAR
Entrez Id: 80055
Gene Symbol: PGAP1
PGAP1 		0.600 Biomarker disease CTD_human
Entrez Id: 51185
Gene Symbol: CRBN
CRBN 		0.200 Biomarker disease MGD Rescue of Learning and Memory Deficits in the Human Nonsyndromic Intellectual Disability Cereblon Knock-Out Mouse Model by Targeting the AMP-Activated Protein Kinase-mTORC1 Translational Pathway. 29459374 2018
Entrez Id: 51185
Gene Symbol: CRBN
CRBN 		0.200 Biomarker disease MGD Behavioral characterization of cereblon forebrain-specific conditional null mice: a model for human non-syndromic intellectual disability. 21995942 2012